FILTEK SUPREME ULTRA FLOWABLE RESTORATIVE
K-Number: K100235 · 2010-05-12
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Device Summary
Frequently Asked Questions
What is the FILTEK SUPREME ULTRA FLOWABLE RESTORATIVE?
FILTEK SUPREME ULTRA FLOWABLE RESTORATIVE is a medical device that received FDA 510(k) clearance on 2010-05-12. The listed applicant is 3M Company. The 510(k) number is K100235.
When did FILTEK SUPREME ULTRA FLOWABLE RESTORATIVE receive FDA 510(k) clearance?
FILTEK SUPREME ULTRA FLOWABLE RESTORATIVE received FDA 510(k) clearance on 2010-05-12, under 510(k) number K100235.
Who is the listed applicant for FILTEK SUPREME ULTRA FLOWABLE RESTORATIVE?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FILTEK SUPREME ULTRA FLOWABLE RESTORATIVE?
The FDA product code for FILTEK SUPREME ULTRA FLOWABLE RESTORATIVE is EBF.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing 3M Company as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: EBF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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